510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K954953Unknown

B-D Durasafe Combined Spinal Epidural (Cse) Tray

BD Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lake NJ / Traditional, Unknown
FDA source (opens on fda.gov)

K954953 is the FDA 510(k) clearance record for B-D DURASAFE COMBINED SPINAL EPIDURAL (CSE) TRAY, a class II device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code CAZ (Anesthesia Conduction Kit). FDA's definition for product code CAZ reads: "This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the...". FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K954953.

Clearance record

Decision date
Received
(203 days to decision)
Product code
CAZ Anesthesia Conduction Kit
Regulation
21 CFR 868.5140
Device class
Class II
Review panel
Anesthesiology
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic One Becton Dr., Franklin Lake NJ
510(k) summary
Summary
Third party review
No

Clearances, product code CAZ

Trailing 12 months
1 clearance under product code CAZ in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260